›› 2023, Vol. 37 ›› Issue (7): 34-40.

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姜黄素-聚乙烯醇药物凝胶的制备及性能研究

王培,牛丽丽,陈灵智   

  1. 衡水学院
  • 收稿日期:2023-03-03 修回日期:2023-03-28 出版日期:2023-07-26 发布日期:2023-07-26
  • 基金资助:
    衡水市教育科学研究“十四五”规划课题;大学生创新创业训练计划项目

Preparation and properties of curcumin-polyvinyl alcohol drug hydrogel

  • Received:2023-03-03 Revised:2023-03-28 Online:2023-07-26 Published:2023-07-26

摘要: 以姜黄素为原药、聚乙烯醇为载体,制备了具有缓释性的姜黄素-聚乙烯醇药物凝胶。通过平衡溶胀度和红外对凝胶进行了表征;采用单因素和响应面法,考察了药物凝胶载药量的影响因素;通过标准曲线考察了药物凝胶的缓释性。结果表明,相同条件下,在40 ℃凝胶的溶胀度最大,为(171.53±0.21) %,红外表征表明该凝胶可进行后续实验;单因素法表明,姜黄素初始浓度为70 μg/mL、时间为1.5 h和温度为40 ℃时,凝胶载药量达到最大为(43.43±0.243 2) mg/g;响应面法分析结果表明,姜黄素的初始浓度对载药量影响最显著,其次为温度,而吸附时间对载药量影响相对较小;在PBS缓冲液中,16 h内姜黄素累计释放率达到88.1 %,释药行为接近一级方程,表明制得的药物凝胶具有一定的缓释作用。

关键词: 姜黄素, 聚乙烯醇, 凝胶, 响应面, 缓释

Abstract: A type of controlled-release drug hydrogels was prepared with curcumin as an original drug and polyvinyl alcohol as a carrier. The structure and performance of the as-prepared drug hydrogels were characterized by using balanced swelling and Fourier-transform infrared spectroscopy. The effects of drug-loading of the hydrogels were investigated by using the single factor and response surface methods, and the controlled-release properties of the drug hydrogels were evaluated through a standard curve. The experimental results indicated that the hydrogels obtained a maximum swelling rate of (171.53±0.21) % at 40 oC under the same conditions. Based on the single-factor method, the drug-loading of the hydrogels reached a maximum of (43.43±0.243 2) mg/g at 40 oC for 1.5 h under the initial curcumin concentration of 70 μg/mL. The results from the response surface analysis indicated that the initial concentration of curcumin generated the most significant effect on the drug-loading, followed with temperature. However, the adsorption time only had a relatively small effect on the drug-loading. In the phosphate buffered solution, the cumulative release rate of curcumin reached 88.1 %, indicating a certain controlled-release effect of the drug hydrogels.

Key words: curcumin, polyvinyl alcohol, hydrogel, response surface analysis, controlled-release